US20120308505A1 - Clear Hair Care Composition Comprising Base Oil and Hydrophilic Component - Google Patents
Clear Hair Care Composition Comprising Base Oil and Hydrophilic Component Download PDFInfo
- Publication number
- US20120308505A1 US20120308505A1 US13/482,213 US201213482213A US2012308505A1 US 20120308505 A1 US20120308505 A1 US 20120308505A1 US 201213482213 A US201213482213 A US 201213482213A US 2012308505 A1 US2012308505 A1 US 2012308505A1
- Authority
- US
- United States
- Prior art keywords
- composition
- alcohol
- hair care
- care composition
- base oil
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 116
- 239000002199 base oil Substances 0.000 title claims abstract description 21
- 239000007788 liquid Substances 0.000 claims abstract description 35
- 150000002191 fatty alcohols Chemical class 0.000 claims abstract description 30
- 150000001875 compounds Chemical class 0.000 claims abstract description 28
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 27
- 239000000463 material Substances 0.000 claims abstract description 26
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 13
- 239000002480 mineral oil Substances 0.000 claims abstract description 13
- 235000010446 mineral oil Nutrition 0.000 claims abstract description 10
- 230000003750 conditioning effect Effects 0.000 claims description 22
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 claims description 15
- 229940101267 panthenol Drugs 0.000 claims description 15
- 235000020957 pantothenol Nutrition 0.000 claims description 15
- 239000011619 pantothenol Substances 0.000 claims description 15
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 10
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 claims description 8
- MRAMPOPITCOOIN-VIFPVBQESA-N (2r)-n-(3-ethoxypropyl)-2,4-dihydroxy-3,3-dimethylbutanamide Chemical compound CCOCCCNC(=O)[C@H](O)C(C)(C)CO MRAMPOPITCOOIN-VIFPVBQESA-N 0.000 claims description 4
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 claims description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims description 4
- 229940043348 myristyl alcohol Drugs 0.000 claims description 4
- 229940055577 oleyl alcohol Drugs 0.000 claims description 4
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 claims description 4
- 229940023735 panthenyl ethyl ether Drugs 0.000 claims description 4
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 claims description 3
- 239000000047 product Substances 0.000 description 19
- 229920013822 aminosilicone Polymers 0.000 description 15
- 230000008901 benefit Effects 0.000 description 14
- 239000003921 oil Substances 0.000 description 11
- 235000019198 oils Nutrition 0.000 description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- -1 siloxanes Chemical class 0.000 description 5
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 description 4
- 239000011707 mineral Substances 0.000 description 4
- 235000010755 mineral Nutrition 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 3
- 229940057905 laureth-3 Drugs 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 230000003381 solubilizing effect Effects 0.000 description 3
- 239000013638 trimer Substances 0.000 description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 description 3
- 239000008158 vegetable oil Substances 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- FKMHSNTVILORFA-UHFFFAOYSA-N 2-[2-(2-dodecoxyethoxy)ethoxy]ethanol Chemical compound CCCCCCCCCCCCOCCOCCOCCO FKMHSNTVILORFA-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 0 C.C.[93*][SiH]([93*])(C)(C)O[SiH]([93*])([93*])(C)O[SiH]([93*])([93*])(C)C Chemical compound C.C.[93*][SiH]([93*])(C)(C)O[SiH]([93*])([93*])(C)O[SiH]([93*])([93*])(C)C 0.000 description 2
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000019485 Safflower oil Nutrition 0.000 description 2
- YFCGDEUVHLPRCZ-UHFFFAOYSA-N [dimethyl(trimethylsilyloxy)silyl]oxy-dimethyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C YFCGDEUVHLPRCZ-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000003289 ascorbyl group Chemical class [H]O[C@@]([H])(C([H])([H])O*)[C@@]1([H])OC(=O)C(O*)=C1O* 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 230000001143 conditioned effect Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- NFVSFLUJRHRSJG-UHFFFAOYSA-N hexadecamethylheptasiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C NFVSFLUJRHRSJG-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 2
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 235000005713 safflower oil Nutrition 0.000 description 2
- 239000003813 safflower oil Substances 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 210000004761 scalp Anatomy 0.000 description 2
- 210000002374 sebum Anatomy 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 229940032094 squalane Drugs 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- 239000002888 zwitterionic surfactant Substances 0.000 description 2
- HDTRYLNUVZCQOY-UHFFFAOYSA-N α-D-glucopyranosyl-α-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OC1C(O)C(O)C(O)C(CO)O1 HDTRYLNUVZCQOY-UHFFFAOYSA-N 0.000 description 1
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- 229940015975 1,2-hexanediol Drugs 0.000 description 1
- 150000000211 1-dodecanols Chemical class 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- MSWZFWKMSRAUBD-IVMDWMLBSA-N 2-amino-2-deoxy-D-glucopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 description 1
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
- QGXLVXZRPRRCRP-IDIVVRGQSA-L Adenosine 5'-phosphate disodium Chemical compound [Na+].[Na+].C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP([O-])([O-])=O)[C@@H](O)[C@H]1O QGXLVXZRPRRCRP-IDIVVRGQSA-L 0.000 description 1
- 241000195940 Bryophyta Species 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 235000004866 D-panthenol Nutrition 0.000 description 1
- 239000011703 D-panthenol Substances 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 206010019049 Hair texture abnormal Diseases 0.000 description 1
- 102000011782 Keratins Human genes 0.000 description 1
- 108010076876 Keratins Proteins 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
- 229920000604 Polyethylene Glycol 200 Polymers 0.000 description 1
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 1
- 229920002582 Polyethylene Glycol 600 Polymers 0.000 description 1
- 229920002385 Sodium hyaluronate Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- HDTRYLNUVZCQOY-WSWWMNSNSA-N Trehalose Natural products O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-WSWWMNSNSA-N 0.000 description 1
- 206010044625 Trichorrhexis Diseases 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- HDTRYLNUVZCQOY-LIZSDCNHSA-N alpha,alpha-trehalose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 HDTRYLNUVZCQOY-LIZSDCNHSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- FEOYLBRDNMCIHQ-UHFFFAOYSA-N carbonic acid;pyrrolidin-2-one Chemical compound OC(O)=O.O=C1CCCN1 FEOYLBRDNMCIHQ-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- KXKPYJOVDUMHGS-OSRGNVMNSA-N chondroitin sulfate Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](OS(O)(=O)=O)[C@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](C(O)=O)O1 KXKPYJOVDUMHGS-OSRGNVMNSA-N 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 229960003949 dexpanthenol Drugs 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 229960002442 glucosamine Drugs 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000002303 glucose derivatives Chemical class 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 1
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- ZCTXEAQXZGPWFG-UHFFFAOYSA-N imidurea Chemical compound O=C1NC(=O)N(CO)C1NC(=O)NCNC(=O)NC1C(=O)NC(=O)N1CO ZCTXEAQXZGPWFG-UHFFFAOYSA-N 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 125000000627 niacin group Chemical class 0.000 description 1
- 229960003966 nicotinamide Drugs 0.000 description 1
- 239000011570 nicotinamide Substances 0.000 description 1
- 235000005152 nicotinamide Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 229920002523 polyethylene Glycol 1000 Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- YNZOICUNEVJUEJ-UHFFFAOYSA-N propane-1,2,3-triol Chemical compound OCC(O)CO.OCC(O)CO.OCC(O)CO YNZOICUNEVJUEJ-UHFFFAOYSA-N 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 229930195734 saturated hydrocarbon Chemical group 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229940010747 sodium hyaluronate Drugs 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- YWIVKILSMZOHHF-QJZPQSOGSA-N sodium;(2s,3s,4s,5r,6r)-6-[(2s,3r,4r,5s,6r)-3-acetamido-2-[(2s,3s,4r,5r,6r)-6-[(2r,3r,4r,5s,6r)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2- Chemical compound [Na+].CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 YWIVKILSMZOHHF-QJZPQSOGSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
- 229940043810 zinc pyrithione Drugs 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/31—Hydrocarbons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
Definitions
- the present invention relates to a non-aqueous clear hair care composition
- a non-aqueous clear hair care composition comprising: a base oil consisting of an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof; an hydrophilic material; and a liquid fatty alcohol having 10 carbon atoms or more; wherein the weight ratio of the hydrophilic material to the liquid fatty alcohol is from about 1:70 to about 1:800.
- shampooing cleans the hair by removing excess soil and sebum.
- shampooing can leave the hair in a wet, tangled, and generally unmanageable state. Once the hair dries, it is often left in a dry, rough, lusterless, or frizzy condition due to removal of the hair's natural oils and other natural conditioning and moisturizing components.
- the hair can further be left with increased levels of static upon drying, which can interfere with combing and result in a condition commonly referred to as “fly-away hair,” or contribute to an undesirable phenomenon of “split ends.”
- chemical treatments such as perming, bleaching, or coloring hair, can also damage hair and leave it dry, rough, lusterless, and damaged.
- Conditioning formulations can be in the form of rinse-off products or leave-on products, and can be in the form of an emulsion, cream, gel, spray, mousse, oil, liquid and serum.
- compositions comprising 2.0% panthenol, 8.0% polyethylene glycol 400, 10% 1-dodecanol, 10% isopropyl palmitate, and 61.7% safflower oil.
- This US publication discloses in Example No. 13 a composition comprising 2.0% panthenol, 8.0% dipropylene glycol 400, 30% 1-dodecanol, 10% isopropyl palmitate, and 41.7% squalane.
- the US publication further discloses in Comparative Examples, compositions comprising 2.0% panthenol, 30% oleyl alcohol, 10% isopropyl palmitate, and 41.7% squalane.
- a hair and scalp treating composition comprising: 0.01-99.99 wt % of an oil selected from the group consisting of silicone oils, hydrocarbon oils, fluorocarbon oils, vegetable oils, mineral oils, and mixtures thereof; 0.0001-50 wt % of a polar active ingredient selected from water soluble B complex vitamins; 0.001-50 wt % of a surface active agent selected from the group consisting of anionic surfactants, cationic surfactants, amphoteric surfactants, zwitterionic surfactants, nonionic surfactants, and mixtures thereof.
- Example IV a hair oil composition (water-in-oil emulsion) comprising a total 60% mineral oil, q.s. to 100% grandnut oil and 0.001% panthenol, 0.009% panthenyl ethyl ether, and 2% laureth-3.
- the present invention is directed to a non-aqueous clear hair care composition comprising by weight:
- a base oil consisting of: an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof; from about 0.0005% to about 0.1% of an hydrophilic material; from about 0.035% to about 15% of a liquid fatty alcohol having 10 carbon atoms or more; wherein the weight ratio of the hydrophilic material to the liquid fatty alcohol is from about 1:70 to about 1:800.
- the hair care compositions of the present invention provide reduced greasy feel, while solubilizing hydrophilic components such as panthenol.
- mixtures is meant to include a simple combination of materials and any compounds that may result from their combination.
- composition of the present invention is a non-aqueous clear hair care composition comprising by weight:
- a base oil consisting of: an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof; from about 0.0005% to about 0.1% of an hydrophilic material; from about 0.035% to about 15% of a liquid fatty alcohol having 10 carbon atoms or more; wherein the weight ratio of the hydrophilic material to the liquid fatty alcohol is from about 1:70 to about 1:800.
- the composition when the composition comprises the above base oil at the above level, the composition provides reduced sticky/greasy feel, compared to other base oils such as those containing a larger amount of vegetable oils including safflower oil.
- other base oils such as those containing a larger amount of vegetable oils including safflower oil.
- hydrophilic materials such as panthenol in the composition.
- the inventors of the present invention have found that, by the addition of specific liquid alcohol at a specific ratio, hydrophilic materials are dissolved in the composition comprising the above base oil, and the composition has a clear product appearance.
- the composition of the present invention is a non-aqueous composition.
- Non-aqueous composition herein means that the composition is substantially free of water.
- the composition being substantially free of water means that: the composition is free of water; or, if the composition contains water, the level of water is very low.
- the level of water if included, 1% or less, preferably 0.5% or less, more preferably 0.3% or less, still more preferably 0.1% or less, even more preferably 0% by weight of the composition.
- composition of the present invention has a homogeneous clear product appearance, i.e., homogeneous transparent product appearance.
- the composition of the present invention has a turbidity of 2.0NTU or less, 1.5NTU or less, more preferably 1.0NTU or less, still more preferably 0.7NTU or less at 25° C. Further preferably, the composition of the present invention has such above turbidity at 25° C., even after its storage at 5° C. for at least 1 hour.
- the transmittances are measured by using HACH 2100N Turbidimeter.
- substantially insoluble compound, what is meant is that: the compound is substantially insoluble in the compositions at the level used; and,
- compositions when containing the compounds at the level used, are either: (i) non-homogeneous by, for example, phase separation; or (ii) homogeneous but with a higher turbidity, i.e., turbidity of above 2.0NTU (excluding 2.0NTU), preferably above 1.5NTU (excluding 1.5NTU), more preferably above 1.0NTU (excluding 1.0NTU), still more preferably above 0.7NTU (excluding 0.7NTU) at 25° C.
- turbidity i.e., turbidity of above 2.0NTU (excluding 2.0NTU), preferably above 1.5NTU (excluding 1.5NTU), more preferably above 1.0NTU (excluding 1.0NTU), still more preferably above 0.7NTU (excluding 0.7NTU) at 25° C.
- Such substantially insoluble compounds further include fatty compounds including, for example: fatty alcohols having a melting point of 25° C. or more, such as cetyl alcohol and stearyl alcohol; fatty acids having a melting point of 25° C. or more, such as stearic acid; fatty alcohol derivatives and fatty acid derivatives such as esters and ethers thereof, which derivatives have a melting point of 25° C. or more; and mixtures thereof.
- fatty compounds including, for example: fatty alcohols having a melting point of 25° C. or more, such as cetyl alcohol and stearyl alcohol; fatty acids having a melting point of 25° C. or more, such as stearic acid; fatty alcohol derivatives and fatty acid derivatives such as esters and ethers thereof, which derivatives have a melting point of 25° C. or more; and mixtures thereof.
- such substantially insoluble compounds further include, fatty alcohol derivatives, fatty acids, and fatty acid derivatives, those having a lower melting point than 25° C.
- the compositions of the present invention are substantially free of such substantially insoluble compounds.
- the compositions being “substantially free” of substantially insoluble compounds means that: the composition is free of substantially insoluble compounds; or, if the composition contains substantially insoluble compounds, the level of such substantially insoluble compounds is very low. In the present invention, the level of such substantially insoluble compounds is, if included, 1.0% or less, preferably 0.5% or less, more preferably 0.3% or less, still more preferably 0.1% or less, even more preferably 0%.
- composition of the present invention is substantially free of surfactants, in view of product clarity and/or reduced undesirable foaming of the product.
- Such surfactants include: anionic surfactants; cationic surfactants; amphoteric surfactants; zwitterionic surfactants; nonionic surfactants having a HLB of 5 or more; and mixtures thereof.
- nonionic surfactants having a HLB of 5 or more includes, for example: ethers of fatty alcohols such as ethers of lauryl alcohol including Laureth-3 (having a HLB of about 8); esters of fatty alcohols such as esters of lauryl alcohols.
- the composition being substantially free of surfactants means that: the composition is free of surfactants; or, if the composition contains surfactants, the level of such surfactants is very low.
- the total level of such surfactants is, if included, preferably 0.1% or less, more preferably 0.01% or less, still more preferably 0.001% or less, even more preferably 0.0005% by weight of the composition.
- the composition of the present invention comprises a base oil.
- the base oil is included at a level by weight of the composition of, from about 61% to about 99.9%, from about 70% to about 99.5%, more preferably from about 75% to about 99.0%, still more preferably from about 80% to about 98%, still more preferably from about 85% to about 98%.
- the base oil useful herein consists of an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof.
- the base oil consists of an isoparaffin, a mineral oil, and mixtures thereof, in view of balance between reduced sticky/greasy feel and conditioned feel which could be delivered by a higher viscosity.
- the isoparaffins useful herein have a viscosity of, preferably from about 0.5 mm 2 ⁇ s ⁇ 1 to about 50 mm 2 ⁇ s ⁇ 1 , more preferably from about 0.8 mm 2 ⁇ s ⁇ 1 to about 40 mm 2 ⁇ s ⁇ 1 , still more preferably from about 1 mm 2 ⁇ s ⁇ 1 to about 30 mm 2 ⁇ s ⁇ 1 , even more preferably from about 1.5 mm 2 ⁇ s ⁇ 1 to about 20 mm 2 ⁇ s ⁇ 1 , further more preferably from about 1.5 mm 2 ⁇ s ⁇ 1 to about 10 mm 2 ⁇ s ⁇ 1 at 37.8° C.
- the mixture of isoparaffin have the above viscosity.
- Isoparaffins useful herein are preferably volatile.
- the volatile isoparaffin useful herein are those having from about 8 to about 20 carbon atoms, more preferably from about 8 to about 16 carbon atoms, still more preferably from about 8 to about 12 carbon atoms, even more preferably from about 10 to about 12 carbon atoms.
- preferred isoparaffin include, for example, trimer, tetramer, pentamer, and hexamer of isobutene, and mixtures thereof.
- Commercially available isoparaffin may have distributions of its polymerization degree, and may be mixtures of, for example, trimer, tetramer, pentamer, and hexamer.
- tetramer herein is that a commercially available isoparaffin hydrocarbons in which tetramer has the highest content, i.e., tetramer is included at a level of preferably 70% or more, more preferably 80% or more, still more preferably 85% or more.
- the mineral oils useful herein are those having a viscosity of, preferably from about 0.5 mm 2 ⁇ s ⁇ 1 to about 130 mm 2 ⁇ s ⁇ 1 , more preferably from about 0.8 mm 2 ⁇ s ⁇ 1 to about 120 mm 2 ⁇ s ⁇ 1 , still more preferably from about 1 mm 2 ⁇ s ⁇ 1 to about 100 mm 2 ⁇ s ⁇ 1 , even more preferably from about 1.5 mm 2 ⁇ s ⁇ 1 to about 90 mm 2 ⁇ s ⁇ 1 , at 37.8° C.
- the mineral oils useful herein are non-volatile and/or those having from about 18 to about 60 carbon atoms, more preferably from about 20 to about 50 carbon atoms, still more preferably from about 20 to about 40 carbon atoms.
- volatile silicone compounds useful herein include polyalkyl or polyaryl siloxanes with the following structure (I):
- R 93 is independently alkyl or aryl, and x is an integer from about 0 to about 5.
- Z 8 represents groups which block the ends of the silicone chains.
- R 93 groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl
- Z 8 groups include hydroxy, methyl, methoxy, ethoxy, propoxy, and aryloxy. More preferably, R 93 groups and Z 8 groups are methyl groups.
- the preferred volatile silicone compounds are hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, hexadecamethylheptasiloxane.
- volatile silicone compounds useful herein include octamethyltrisiloxane with tradename SH200C-1cs, decamethyltetrasiloxane with tradename SH200C-1.5 cs, hexadecamethylheptasiloxane with tradename SH200C-2cs, all available from Dow Corning.
- volatile silicone compounds useful herein also include a cyclic silicone compound having the formula:
- R 93 is independently alkyl or aryl, and n is an integer of from 3 to 7.
- R 93 groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl. More preferably, R 93 groups are methyl groups.
- the preferred volatile silicone compounds are octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, tetradecamethylcyclohexasiloxane.
- Commercially available volatile silicone compounds useful herein include octamethylcyclotetrasiloxane with tradename SH244, decamethylcyclopentasiloxane with tradename DC 345 all available from Dow Corning.
- the composition of the present invention comprises a hydrophilic material.
- the hydrophilic material is included at a level by weight of the composition of, from about 0.0005% to about 0.1%, preferably from about 0.001% to about 0.07%, more preferably from about 0.03% to about 0.05%.
- the hydrophilic materials include, for example, panthenol, panthenyl ethyl ether, water-soluble plant extracts, Vitamin B 3 compounds such as niacinamide, Ascorbic acid compounds such as Ascorbyl glucosid, Peptides, hydrophilic polyols and mixtures thereof.
- Hydrophilic polyols contain, for example, glycerin diglycerin, propylene glycol, dipropylene glycol, butylene glycol, hexylene glycol, sorbitol, ethoxylated glucose, 1,2-hexane diol, hexanetriol, erythritol, trehalose, xylitol, maltitol, maltose, glucose, fructose, sodium chondroitin sulfate, sodium hyaluronate, sodium adenosin phosphate, sodium lactate, pyrrolidone carbonate, glucosamine, cyclodextrin, and mixtures thereof.
- glycerin diglycerin propylene glycol, dipropylene glycol, butylene glycol, hexylene glycol, sorbitol, ethoxylated glucose, 1,2-hexane diol, hexanetriol, erythr
- Hydrophilic polyols also include water-soluble alkoxylated nonionic polymers such as polyethylene glycols and polypropylene glycols having a molecular weight of up to about 1000 such as those with CTFA names PEG-200, PEG-400, PEG-600, PEG-1000, and mixtures thereof.
- hydrophilic materials preferred are those selected from the group consisting of panthenol, panthenyl ethyl ether, and mixtures thereof.
- the composition of the present invention comprises a liquid fatty alcohol.
- the liquid fatty alcohol is included at a level by weight of the composition of, from about 0.035% to about 15%, preferably from about 0.1% to about 10%, more preferably from about 0.3% to about 7%.
- the liquid fatty alcohol is included at a level such that the weight ratio of the hydrophilic material to the liquid fatty alcohol is 1:70 to about 1:800, preferably from about 1:85 to about 1:600, more preferably from about 1:100 to about 1:350, in view of dissolving the hydrophilic material.
- the composition may have at least one of the following tendencies: increased sticky feel, less conditioned feel, undesirable foaming during usage and/or transportation, and reduced stability at lower temperature.
- liquid fatty alcohols useful herein are those having 10 carbon atoms or more, and are liquid at 25° C.
- such liquid fatty alcohols have a melting point of 25° C. or lower, more preferably 20° C. or lower.
- the liquid fatty alcohols useful herein include, for example: lauryl alcohol; a mixture of lauryl alcohol and myristyl alcohol; oleyl alcohol; isocetyl alcohol; isostearyl alcohol; and mixtures thereof.
- the liquid fatty alcohol is selected from the group consisting of: lauryl alcohol; and a mixture of lauryl alcohol and myristyl alcohol, in view of its solubility in the base oil and its solubility of panthenol.
- the composition of the present invention can contain a silicone conditioning agent.
- the silicone conditioning agent can be included at a level by weight of the composition of, preferably from about 0.1%, more preferably from about 0.2%, still more preferably from about 0.5% in view of providing dry conditioning benefit such as reduced friction, and preferably to about 15%, more preferably to about 10%, still more preferably to about 8%, even more preferably to about 5% in view of conditioning benefits and/or product clarity.
- the silicone conditioning agents useful herein are non-volatile, and preferably liquid at 25° C.
- the silicone conditioning agents useful herein have an apparent viscosity of, preferably from about 200 to about 300,000 mm 2 ⁇ s ⁇ 1 , more preferably from about 200 to about 50,000 mm 2 ⁇ s ⁇ 1 , at 25° C., in view of providing conditioning benefits.
- silicone conditioning agents useful herein are hydrophobic and those having a HLB of about 8 or less, preferably 5 or less.
- the silicone conditioning agents useful herein are, preferably, in non-emulsion form.
- the silicone conditioning agent is preferably an aminosilicone.
- aminosilicones useful herein have an amine content of less than about 0.12 m mol/g, more preferably less than about 0.1 m mol/g, still more preferably less than about 0.08 m mol/g, even more preferably less than about 0.06 m mol/g, in view of friction reduction benefit. It has been surprisingly found that higher levels of nitrogen (amine functional groups) in the amino silicone tend to result in less friction reduction, and consequently less conditioning benefit from the aminosilicone.
- Aminosilicone useful herein are those which conform to the general formula (I):
- G is hydrogen, phenyl, hydroxy, or C 1 -C 8 alkyl, preferably methyl; a is an integer having a value from 1 to 3, preferably 1; b is 0, 1 or 2, preferably 1; n is a number from 1 to 2,000, preferably from 100 to 1,800, more preferably from 300 to 800, still more preferably 500-600; m is 0; R 1 is a monovalent radical conforming to the general formula CqH 2q L, wherein q is an integer having a value from 2 to 8 and L is selected from the following groups: —N(R 2 )CH 2 —CH 2 —N(R 2 ) 2 ; —N(R 2 ) 2 ; —N(R 2 ) 3 A ⁇ ; —N(R 2 )CH 2 —CH 2 —NR 2 H 2 A ⁇ ; wherein R 2 is hydrogen, phenyl, benzyl, or a saturated hydrocarbon radical, preferably an alkyl radical from about C
- Such preferred aminosilicones can be called as terminal aminosilicones, as one or both ends of the silicone chain are terminated by nitrogen containing group. It is also surprisingly found that, such terminal aminosilicones provide improved friction reduction compared to graft aminosilicones.
- composition of the present invention may include other additional components, which may be selected by the artisan according to the desired characteristics of the final product and which are suitable for rendering the composition more cosmetically or aesthetically acceptable or to provide them with additional usage benefits.
- additional components generally are used individually at levels of from about 0.001% to about 10%, preferably up to about 5% by weight of the composition.
- compositions can be formulated into the present compositions. These include: other conditioning agents such as hydrolysed collagen with tradename Peptein 2000 available from Hormel, vitamin E with tradename Emix-d available from Eisai, hydrolysed keratin, proteins, and nutrients; preservatives such as benzyl alcohol, methyl paraben, propyl paraben and imidazolidinyl urea; coloring agents, such as any of the FD&C or D&C dyes; perfumes; and antidandruff agents such as zinc pyrithione and salicylic acid.
- other conditioning agents such as hydrolysed collagen with tradename Peptein 2000 available from Hormel, vitamin E with tradename Emix-d available from Eisai, hydrolysed keratin, proteins, and nutrients
- preservatives such as benzyl alcohol, methyl paraben, propyl paraben and imidazolidinyl urea
- coloring agents such as any of the FD&C or D&C dyes
- perfumes and
- the hair care compositions of the present invention can be hair conditioning and/or hair styling products, and the like.
- the hair care compositions of the present invention are, preferably, in the form of leave-on products.
- the hair care compositions of the present invention can be formulated in a wide variety of product forms, including but not limited to gels, sprays, oils, liquid and serum.
- the compositions of the present invention are in a liquid form such as oil, liquid and serum.
- the hair care composition is preferably applied to wet or damp hair prior to drying of the hair. After such hair care compositions are applied to the hair, the hair is dried and styled in accordance with the preference of the user. In the alternative, it may be applied to already dry hair, and the hair is then combed or styled, and dried in accordance with the preference of the user.
- Volatile Isoparaffin Trimer of isobutene having a viscosity of 1.4 mm 2 ⁇ s ⁇ 1 at 37.8° C.
- Non-volatile mineral oil-1 Having a viscosity of about 11-14 mm 2 ⁇ s ⁇ 1 at 37.8° C.
- Non-volatile mineral oil-2 Having a viscosity of about 70 mm 2 ⁇ s ⁇ 1 at 37.8° C.
- Terminal aminosilicone which is available from GE having a viscosity of about 10,000 mm 2 ⁇ s ⁇ 1 at 25° C., and having following formula: (R 1 ) a G 3 ⁇ a —Si—(—OSiG 2 ) n —(—OSiG b (R 1 ) 2 ⁇ b ) m —O—SiG 3 ⁇ a (R 1 ) a
- G is methyl
- a is an integer of 1
- n is a number from 400 to about 600
- m is an integer of 0
- R 1 is a monovalent radical conforming to the general formula CqH 2q L, wherein q is an integer of 3 and L is —NH 2
- compositions of “Ex. 1” through “Ex. 4” and “Ex. i” through “Ex. iii” as shown above can be prepared by any conventional method well known in the art. They are suitably made as follows:
- Hydrophilic materials such as panthenol and liquid fatty alcohols are added to the base oil with agitation at room temperature until homogenized. If included, other components such as silicones and perfumes are added to the mixture with agitation.
- Turbidity is measured by the method described above.
- stickiness/greasiness are evaluated by the following methods. The results of the evaluation are shown above.
- Examples 1 through 4 are hair conditioning compositions of the present invention which are particularly useful for leave-on use.
- the embodiments disclosed and represented by the previous “Ex. 1” through “Ex. 4” have many advantages. For example, they provide reduced greasy feel while solubilizing hydrophilic components such as panthenol, and have a homogeneous clear product appearance. Such advantages can be understood by the comparison between the examples of the present invention and comparative examples “Ex. i” through “Ex. iii”.
- the compositions of the comparative examples “Ex. i” and “Ex. iii” does not have clear product appearance.
- the composition of the comparative example “Ex. ii” has increased stickiness/greasiness, compared to the compositions “Ex. 1” through “Ex. 3” of the present invention.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Disclosed is a non-aqueous clear hair care composition comprising by weight: from about 61% to about 99.9% of a base oil consisting of: an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof; from about 0.0005% to about 0.1% of an hydrophilic material; from about 0.035% to about 15% of a liquid fatty alcohol having 10 carbon atoms or more; wherein the weight ratio of the hydrophilic material to the liquid fatty alcohol is from about 1:70 to about 1:800. By the use of liquid fatty alcohol, hydrophilic materials are dissolved in the base oil and the composition has a clear product appearance.
Description
- This application claims the benefit of U.S. Provisional Application No. 61/492,843 filed on Jun. 3, 2011.
- The present invention relates to a non-aqueous clear hair care composition comprising: a base oil consisting of an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof; an hydrophilic material; and a liquid fatty alcohol having 10 carbon atoms or more; wherein the weight ratio of the hydrophilic material to the liquid fatty alcohol is from about 1:70 to about 1:800. By the use of liquid fatty alcohol, hydrophilic materials are dissolved in the base oil and the composition has a clear product appearance.
- Human hair becomes soiled due to its contact with the surrounding environment and from the sebum secreted by the scalp. The soiling of hair causes it to have a dirty feel and an unattractive appearance. The soiling of the hair necessitates shampooing with frequent regularity.
- Shampooing cleans the hair by removing excess soil and sebum. However, shampooing can leave the hair in a wet, tangled, and generally unmanageable state. Once the hair dries, it is often left in a dry, rough, lusterless, or frizzy condition due to removal of the hair's natural oils and other natural conditioning and moisturizing components. The hair can further be left with increased levels of static upon drying, which can interfere with combing and result in a condition commonly referred to as “fly-away hair,” or contribute to an undesirable phenomenon of “split ends.” Further, chemical treatments, such as perming, bleaching, or coloring hair, can also damage hair and leave it dry, rough, lusterless, and damaged.
- A variety of approaches have been developed to condition the hair. A common method of providing conditioning benefits to the hair is through the use of application of hair conditioning composition. Conditioning formulations can be in the form of rinse-off products or leave-on products, and can be in the form of an emulsion, cream, gel, spray, mousse, oil, liquid and serum.
- For leave-on products especially those in a non-aqueous liquid form (such as oil, liquid and serum) comprising a larger amount of oily compounds, there was a need for such products to include hydrophilic materials such as panthenol. For example, US 2003/0017179 relates to, according to claim 1, a liquid oil-based cosmetic comprising a main ingredient of at least one kind of animal and vegetable oils, 0.01-6.0 wt % of panthenol, 0.4-10 wt % of a glycol having an average molecular weight of 90-400, and 5-40% of monohydric alcohol having an average molecular weight of 110-250. This US publication discloses in Example No. 10 a composition comprising 2.0% panthenol, 8.0% polyethylene glycol 400, 10% 1-dodecanol, 10% isopropyl palmitate, and 61.7% safflower oil. This US publication discloses in Example No. 13 a composition comprising 2.0% panthenol, 8.0% dipropylene glycol 400, 30% 1-dodecanol, 10% isopropyl palmitate, and 41.7% squalane. The US publication further discloses in Comparative Examples, compositions comprising 2.0% panthenol, 30% oleyl alcohol, 10% isopropyl palmitate, and 41.7% squalane.
- Another example is Australian patent application publication No. AU199642210. This AU publication relates to, according to claim 1, a hair and scalp treating composition comprising: 0.01-99.99 wt % of an oil selected from the group consisting of silicone oils, hydrocarbon oils, fluorocarbon oils, vegetable oils, mineral oils, and mixtures thereof; 0.0001-50 wt % of a polar active ingredient selected from water soluble B complex vitamins; 0.001-50 wt % of a surface active agent selected from the group consisting of anionic surfactants, cationic surfactants, amphoteric surfactants, zwitterionic surfactants, nonionic surfactants, and mixtures thereof. The AU publication discloses in Example IV a hair oil composition (water-in-oil emulsion) comprising a total 60% mineral oil, q.s. to 100% grandnut oil and 0.001% panthenol, 0.009% panthenyl ethyl ether, and 2% laureth-3.
- However, there remains a need for such products which provide reduced greasy feel, while solubilizing hydrophilic components such as panthenol.
- None of the existing art provides all of the advantages and benefits of the present invention.
- The present invention is directed to a non-aqueous clear hair care composition comprising by weight:
- from about 61% to about 99.9% of a base oil consisting of: an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof;
from about 0.0005% to about 0.1% of an hydrophilic material;
from about 0.035% to about 15% of a liquid fatty alcohol having 10 carbon atoms or more;
wherein the weight ratio of the hydrophilic material to the liquid fatty alcohol is from about 1:70 to about 1:800. - The hair care compositions of the present invention provide reduced greasy feel, while solubilizing hydrophilic components such as panthenol.
- These and other features, aspects, and advantages of the present invention will become better understood from a reading of the following description, and appended claims.
- While the specification concludes with claims particularly pointing out and distinctly claiming the invention, it is believed that the present invention will be better understood from the following description.
- Herein, “comprising” means that other steps and other ingredients which do not affect the end result can be added. This term encompasses the terms “consisting of” and “consisting essentially of”.
- All percentages, parts and ratios are based upon the total weight of the compositions of the present invention, unless otherwise specified. All such weights as they pertain to listed ingredients are based on the active level and, therefore, do not include carriers or by-products that may be included in commercially available materials.
- Herein, “mixtures” is meant to include a simple combination of materials and any compounds that may result from their combination.
- The composition of the present invention is a non-aqueous clear hair care composition comprising by weight:
- from about 61% to about 99.9% of a base oil consisting of: an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof;
from about 0.0005% to about 0.1% of an hydrophilic material;
from about 0.035% to about 15% of a liquid fatty alcohol having 10 carbon atoms or more;
wherein the weight ratio of the hydrophilic material to the liquid fatty alcohol is from about 1:70 to about 1:800. - It has been found by the inventor of the present invention that, when the composition comprises the above base oil at the above level, the composition provides reduced sticky/greasy feel, compared to other base oils such as those containing a larger amount of vegetable oils including safflower oil. However, it has been surprisingly found by the inventor of the present invention that, when the composition comprises the above base oil at the above level, it becomes difficult to dissolve hydrophilic materials such as panthenol in the composition.
- The inventors of the present invention have found that, by the addition of specific liquid alcohol at a specific ratio, hydrophilic materials are dissolved in the composition comprising the above base oil, and the composition has a clear product appearance.
- The composition of the present invention is a non-aqueous composition. Non-aqueous composition herein means that the composition is substantially free of water. In the present invention, “the composition being substantially free of water” means that: the composition is free of water; or, if the composition contains water, the level of water is very low. In the present invention, the level of water, if included, 1% or less, preferably 0.5% or less, more preferably 0.3% or less, still more preferably 0.1% or less, even more preferably 0% by weight of the composition.
- The composition of the present invention has a homogeneous clear product appearance, i.e., homogeneous transparent product appearance.
- Preferably, the composition of the present invention has a turbidity of 2.0NTU or less, 1.5NTU or less, more preferably 1.0NTU or less, still more preferably 0.7NTU or less at 25° C. Further preferably, the composition of the present invention has such above turbidity at 25° C., even after its storage at 5° C. for at least 1 hour. The transmittances are measured by using HACH 2100N Turbidimeter.
- In view of homogeneous clear product appearance, it is preferred to control the level of components which are substantially insoluble to the composition of the present invention. By “substantially insoluble” compound, what is meant is that: the compound is substantially insoluble in the compositions at the level used; and,
- when containing the compounds at the level used, the compositions are either: (i) non-homogeneous by, for example, phase separation; or (ii) homogeneous but with a higher turbidity, i.e., turbidity of above 2.0NTU (excluding 2.0NTU), preferably above 1.5NTU (excluding 1.5NTU), more preferably above 1.0NTU (excluding 1.0NTU), still more preferably above 0.7NTU (excluding 0.7NTU) at 25° C.
- Such substantially insoluble compounds further include fatty compounds including, for example: fatty alcohols having a melting point of 25° C. or more, such as cetyl alcohol and stearyl alcohol; fatty acids having a melting point of 25° C. or more, such as stearic acid; fatty alcohol derivatives and fatty acid derivatives such as esters and ethers thereof, which derivatives have a melting point of 25° C. or more; and mixtures thereof.
- When the base oil is a volatile silicone, such substantially insoluble compounds further include, fatty alcohol derivatives, fatty acids, and fatty acid derivatives, those having a lower melting point than 25° C.
- More preferably, the compositions of the present invention are substantially free of such substantially insoluble compounds. In the present invention, the compositions being “substantially free” of substantially insoluble compounds means that: the composition is free of substantially insoluble compounds; or, if the composition contains substantially insoluble compounds, the level of such substantially insoluble compounds is very low. In the present invention, the level of such substantially insoluble compounds is, if included, 1.0% or less, preferably 0.5% or less, more preferably 0.3% or less, still more preferably 0.1% or less, even more preferably 0%.
- Preferably, the composition of the present invention is substantially free of surfactants, in view of product clarity and/or reduced undesirable foaming of the product.
- Such surfactants include: anionic surfactants; cationic surfactants; amphoteric surfactants; zwitterionic surfactants; nonionic surfactants having a HLB of 5 or more; and mixtures thereof. Such nonionic surfactants having a HLB of 5 or more includes, for example: ethers of fatty alcohols such as ethers of lauryl alcohol including Laureth-3 (having a HLB of about 8); esters of fatty alcohols such as esters of lauryl alcohols.
- In the present invention, “the composition being substantially free of surfactants” means that: the composition is free of surfactants; or, if the composition contains surfactants, the level of such surfactants is very low. In the present invention, the total level of such surfactants is, if included, preferably 0.1% or less, more preferably 0.01% or less, still more preferably 0.001% or less, even more preferably 0.0005% by weight of the composition.
- The composition of the present invention comprises a base oil. The base oil is included at a level by weight of the composition of, from about 61% to about 99.9%, from about 70% to about 99.5%, more preferably from about 75% to about 99.0%, still more preferably from about 80% to about 98%, still more preferably from about 85% to about 98%.
- The base oil useful herein consists of an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof. Preferably, the base oil consists of an isoparaffin, a mineral oil, and mixtures thereof, in view of balance between reduced sticky/greasy feel and conditioned feel which could be delivered by a higher viscosity.
- The isoparaffins useful herein have a viscosity of, preferably from about 0.5 mm2·s−1 to about 50 mm2·s−1, more preferably from about 0.8 mm2·s−1 to about 40 mm2·s−1, still more preferably from about 1 mm2·s−1 to about 30 mm2·s−1, even more preferably from about 1.5 mm2·s−1 to about 20 mm2·s−1, further more preferably from about 1.5 mm2·s−1 to about 10 mm2·s−1 at 37.8° C. When using two or more isoparaffin, it is preferred that the mixture of isoparaffin have the above viscosity.
- Isoparaffins useful herein are preferably volatile. Preferably, the volatile isoparaffin useful herein are those having from about 8 to about 20 carbon atoms, more preferably from about 8 to about 16 carbon atoms, still more preferably from about 8 to about 12 carbon atoms, even more preferably from about 10 to about 12 carbon atoms.
- In the present invention, preferred isoparaffin include, for example, trimer, tetramer, pentamer, and hexamer of isobutene, and mixtures thereof. Commercially available isoparaffin may have distributions of its polymerization degree, and may be mixtures of, for example, trimer, tetramer, pentamer, and hexamer. What is meant by tetramer herein is that a commercially available isoparaffin hydrocarbons in which tetramer has the highest content, i.e., tetramer is included at a level of preferably 70% or more, more preferably 80% or more, still more preferably 85% or more.
- The mineral oils useful herein are those having a viscosity of, preferably from about 0.5 mm2·s−1 to about 130 mm2·s−1, more preferably from about 0.8 mm2·s−1 to about 120 mm2·s−1, still more preferably from about 1 mm2·s−1 to about 100 mm2·s−1, even more preferably from about 1.5 mm2·s−1 to about 90 mm2·s−1, at 37.8° C.
- Preferably, the mineral oils useful herein are non-volatile and/or those having from about 18 to about 60 carbon atoms, more preferably from about 20 to about 50 carbon atoms, still more preferably from about 20 to about 40 carbon atoms.
- The volatile silicone compounds useful herein include polyalkyl or polyaryl siloxanes with the following structure (I):
- wherein R93 is independently alkyl or aryl, and x is an integer from about 0 to about 5. Z8 represents groups which block the ends of the silicone chains. Preferably, R93 groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl, Z8 groups include hydroxy, methyl, methoxy, ethoxy, propoxy, and aryloxy. More preferably, R93 groups and Z8 groups are methyl groups. The preferred volatile silicone compounds are hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, hexadecamethylheptasiloxane. Commercially available volatile silicone compounds useful herein include octamethyltrisiloxane with tradename SH200C-1cs, decamethyltetrasiloxane with tradename SH200C-1.5 cs, hexadecamethylheptasiloxane with tradename SH200C-2cs, all available from Dow Corning.
- The volatile silicone compounds useful herein also include a cyclic silicone compound having the formula:
- wherein R93 is independently alkyl or aryl, and n is an integer of from 3 to 7. Preferably, R93 groups include methyl, ethyl, propyl, phenyl, methylphenyl and phenylmethyl. More preferably, R93 groups are methyl groups. The preferred volatile silicone compounds are octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, tetradecamethylcyclohexasiloxane. Commercially available volatile silicone compounds useful herein include octamethylcyclotetrasiloxane with tradename SH244, decamethylcyclopentasiloxane with tradename DC 345 all available from Dow Corning.
- The composition of the present invention comprises a hydrophilic material. The hydrophilic material is included at a level by weight of the composition of, from about 0.0005% to about 0.1%, preferably from about 0.001% to about 0.07%, more preferably from about 0.03% to about 0.05%.
- The hydrophilic materials include, for example, panthenol, panthenyl ethyl ether, water-soluble plant extracts, Vitamin B3 compounds such as niacinamide, Ascorbic acid compounds such as Ascorbyl glucosid, Peptides, hydrophilic polyols and mixtures thereof. Hydrophilic polyols contain, for example, glycerin diglycerin, propylene glycol, dipropylene glycol, butylene glycol, hexylene glycol, sorbitol, ethoxylated glucose, 1,2-hexane diol, hexanetriol, erythritol, trehalose, xylitol, maltitol, maltose, glucose, fructose, sodium chondroitin sulfate, sodium hyaluronate, sodium adenosin phosphate, sodium lactate, pyrrolidone carbonate, glucosamine, cyclodextrin, and mixtures thereof. Hydrophilic polyols also include water-soluble alkoxylated nonionic polymers such as polyethylene glycols and polypropylene glycols having a molecular weight of up to about 1000 such as those with CTFA names PEG-200, PEG-400, PEG-600, PEG-1000, and mixtures thereof.
- Among the hydrophilic materials, preferred are those selected from the group consisting of panthenol, panthenyl ethyl ether, and mixtures thereof.
- The composition of the present invention comprises a liquid fatty alcohol. The liquid fatty alcohol is included at a level by weight of the composition of, from about 0.035% to about 15%, preferably from about 0.1% to about 10%, more preferably from about 0.3% to about 7%. The liquid fatty alcohol is included at a level such that the weight ratio of the hydrophilic material to the liquid fatty alcohol is 1:70 to about 1:800, preferably from about 1:85 to about 1:600, more preferably from about 1:100 to about 1:350, in view of dissolving the hydrophilic material. When the liquid fatty alcohol is included at higher levels than the above ranges, the composition may have at least one of the following tendencies: increased sticky feel, less conditioned feel, undesirable foaming during usage and/or transportation, and reduced stability at lower temperature.
- The liquid fatty alcohols useful herein are those having 10 carbon atoms or more, and are liquid at 25° C. Preferably, such liquid fatty alcohols have a melting point of 25° C. or lower, more preferably 20° C. or lower.
- The liquid fatty alcohols useful herein include, for example: lauryl alcohol; a mixture of lauryl alcohol and myristyl alcohol; oleyl alcohol; isocetyl alcohol; isostearyl alcohol; and mixtures thereof. Preferably, the liquid fatty alcohol is selected from the group consisting of: lauryl alcohol; and a mixture of lauryl alcohol and myristyl alcohol, in view of its solubility in the base oil and its solubility of panthenol.
- The composition of the present invention can contain a silicone conditioning agent. The silicone conditioning agent can be included at a level by weight of the composition of, preferably from about 0.1%, more preferably from about 0.2%, still more preferably from about 0.5% in view of providing dry conditioning benefit such as reduced friction, and preferably to about 15%, more preferably to about 10%, still more preferably to about 8%, even more preferably to about 5% in view of conditioning benefits and/or product clarity.
- The silicone conditioning agents useful herein are non-volatile, and preferably liquid at 25° C. The silicone conditioning agents useful herein have an apparent viscosity of, preferably from about 200 to about 300,000 mm2·s−1, more preferably from about 200 to about 50,000 mm2·s−1, at 25° C., in view of providing conditioning benefits.
- The silicone conditioning agents useful herein are hydrophobic and those having a HLB of about 8 or less, preferably 5 or less.
- The silicone conditioning agents useful herein are, preferably, in non-emulsion form.
- In the present invention, the silicone conditioning agent is preferably an aminosilicone. Preferably, aminosilicones useful herein have an amine content of less than about 0.12 m mol/g, more preferably less than about 0.1 m mol/g, still more preferably less than about 0.08 m mol/g, even more preferably less than about 0.06 m mol/g, in view of friction reduction benefit. It has been surprisingly found that higher levels of nitrogen (amine functional groups) in the amino silicone tend to result in less friction reduction, and consequently less conditioning benefit from the aminosilicone.
- Aminosilicone useful herein are those which conform to the general formula (I):
-
(R1)aG3-a-Si—(—OSiG2)n(—OSiGb(R1)2-b)m—O—SiG3-a(R1)a - wherein G is hydrogen, phenyl, hydroxy, or C1-C8 alkyl, preferably methyl; a is an integer having a value from 1 to 3, preferably 1; b is 0, 1 or 2, preferably 1; n is a number from 1 to 2,000, preferably from 100 to 1,800, more preferably from 300 to 800, still more preferably 500-600; m is 0; R1 is a monovalent radical conforming to the general formula CqH2qL, wherein q is an integer having a value from 2 to 8 and L is selected from the following groups: —N(R2)CH2—CH2—N(R2)2; —N(R2)2; —N(R2)3A−; —N(R2)CH2—CH2—NR2H2A−; wherein R2 is hydrogen, phenyl, benzyl, or a saturated hydrocarbon radical, preferably an alkyl radical from about C1 to about C20; A− is a halide ion. L is preferably —N(CH3)2 or —NH2, more preferably —NH2.
- One highly preferred amino silicones are those corresponding to formula (I) wherein m=0, a=1, q=3, G=methyl, n is preferably from about 1400 to about 1700, more preferably around 1600; and L is —N(CH3)2 or —NH2, more preferably —NH2. Another further highly preferred amino silicones are those corresponding to formula (I) wherein m=0, a=1, q=3, G=methyl, n is preferably from about 400 to about 800, more preferably about 500 to around 600; and L is —N(CH3)2 or —NH2, more preferably —NH2.
- Such preferred aminosilicones can be called as terminal aminosilicones, as one or both ends of the silicone chain are terminated by nitrogen containing group. It is also surprisingly found that, such terminal aminosilicones provide improved friction reduction compared to graft aminosilicones.
- The composition of the present invention may include other additional components, which may be selected by the artisan according to the desired characteristics of the final product and which are suitable for rendering the composition more cosmetically or aesthetically acceptable or to provide them with additional usage benefits. Such other additional components generally are used individually at levels of from about 0.001% to about 10%, preferably up to about 5% by weight of the composition.
- A wide variety of other additional components can be formulated into the present compositions. These include: other conditioning agents such as hydrolysed collagen with tradename Peptein 2000 available from Hormel, vitamin E with tradename Emix-d available from Eisai, hydrolysed keratin, proteins, and nutrients; preservatives such as benzyl alcohol, methyl paraben, propyl paraben and imidazolidinyl urea; coloring agents, such as any of the FD&C or D&C dyes; perfumes; and antidandruff agents such as zinc pyrithione and salicylic acid.
- The hair care compositions of the present invention can be hair conditioning and/or hair styling products, and the like.
- The hair care compositions of the present invention are, preferably, in the form of leave-on products. The hair care compositions of the present invention can be formulated in a wide variety of product forms, including but not limited to gels, sprays, oils, liquid and serum. Preferably, the compositions of the present invention are in a liquid form such as oil, liquid and serum.
- For a leave-on form, the hair care composition is preferably applied to wet or damp hair prior to drying of the hair. After such hair care compositions are applied to the hair, the hair is dried and styled in accordance with the preference of the user. In the alternative, it may be applied to already dry hair, and the hair is then combed or styled, and dried in accordance with the preference of the user.
- The following examples further describe and demonstrate embodiments within the scope of the present invention. The examples are given solely for the purpose of illustration and are not to be construed as limitations of the present invention, as many variations thereof are possible without departing from the spirit and scope of the invention. Where applicable, ingredients are identified by chemical or CTFA name, or otherwise defined below.
-
-
Components Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. i Ex. ii Ex. iii Volatile isoparaffin *1 50.0 50.0 50.0 50.0 50.0 50.0 50.0 Non-volatile mineral oil-1 *2 q.s. to q.s. to q.s. to q.s. to q.s. to q.s. to q.s. to 100% 100% 100% 100% 100% 100% 100% Non-volatile mineral oil-2 *3 10.0 — — — — — — D-Panthenol 0.005 0.005 0.03 0.03 0.03 0.03 0.005 Lauryl alcohol 0.7 0.7 4.0 — 1.0 30.0 — Oleyl alcohol — — — 7.0 — — — Laureth-3 — — — — — — 0.7 Aminosilicone *4 1.0 2.0 2.0 2.0 2.0 2.0 2.0 Perfume 0.4 0.4 0.4 0.4 0.4 0.4 0.4 Turbidity (NTU) at 25° C. 0.4 <2.0 <2.0 <2.0 >5.0 <2.0 >5.0 Stickiness/Greasiness C1 C1 C C1 — X — Definitions of Components *1 Volatile Isoparaffin: Trimer of isobutene having a viscosity of 1.4 mm2 · s−1 at 37.8° C. *2 Non-volatile mineral oil-1: Having a viscosity of about 11-14 mm2 · s−1 at 37.8° C. *3 Non-volatile mineral oil-2: Having a viscosity of about 70 mm2 · s−1 at 37.8° C. *4 Aminosilicone: Terminal aminosilicone which is available from GE having a viscosity of about 10,000 mm2 · s−1 at 25° C., and having following formula: (R1)aG3−a—Si—(—OSiG2)n—(—OSiGb(R1)2−b)m—O—SiG3−a(R1)a wherein G is methyl; a is an integer of 1; n is a number from 400 to about 600; m is an integer of 0; R1 is a monovalent radical conforming to the general formula CqH2qL, wherein q is an integer of 3 and L is —NH2 - The hair conditioning compositions of “Ex. 1” through “Ex. 4” and “Ex. i” through “Ex. iii” as shown above can be prepared by any conventional method well known in the art. They are suitably made as follows:
- Hydrophilic materials such as panthenol and liquid fatty alcohols are added to the base oil with agitation at room temperature until homogenized. If included, other components such as silicones and perfumes are added to the mixture with agitation.
- Turbidity is measured by the method described above. For some of the above compositions, stickiness/greasiness are evaluated by the following methods. The results of the evaluation are shown above.
-
-
- Stickiness/Greasiness is evaluated by 6 panelists, when applying 10 ml of the composition.
- C: Control
- C1: Equal to Control
- X: From 3 to 6 panelists answered that the composition had sticker/greasier feel compared to Control.
- Examples 1 through 4 are hair conditioning compositions of the present invention which are particularly useful for leave-on use. The embodiments disclosed and represented by the previous “Ex. 1” through “Ex. 4” have many advantages. For example, they provide reduced greasy feel while solubilizing hydrophilic components such as panthenol, and have a homogeneous clear product appearance. Such advantages can be understood by the comparison between the examples of the present invention and comparative examples “Ex. i” through “Ex. iii”. For example, the compositions of the comparative examples “Ex. i” and “Ex. iii” does not have clear product appearance. For example, the composition of the comparative example “Ex. ii” has increased stickiness/greasiness, compared to the compositions “Ex. 1” through “Ex. 3” of the present invention.
- The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as “40 mm” is intended to mean “about 40 mm.” The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as “40 mm” is intended to mean “about 40 mm”
- Every document cited herein, including any cross referenced or related patent or application, is hereby incorporated herein by reference in its entirety unless expressly excluded or otherwise limited. The citation of any document is not an admission that it is prior art with respect to any invention disclosed or claimed herein or that it alone, or in any combination with any other reference or references, teaches, suggests or discloses any such invention. Further, to the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govern.
- While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.
Claims (9)
1. A non-aqueous clear hair care composition comprising by weight:
from about 61% to about 99.9% of a base oil consisting of: an isoparaffin, a mineral oil, a volatile silicone compound, and mixtures thereof;
from about 0.0005% to about 0.1% of an hydrophilic material;
from about 0.035% to about 15% of a liquid fatty alcohol having 10 carbon atoms or more;
wherein the weight ratio of the hydrophilic material to the liquid fatty alcohol is from about 1:70 to about 1:800.
2. The hair care composition of claim 1 , wherein the hydrophilic material is selected from the group consisting of panthenol, panthenyl ethyl ether, and mixtures thereof.
3. The hair care composition of claim 1 , wherein the liquid fatty alcohol is selected from the group consisting of: lauryl alcohol; a mixture of lauryl alcohol and myristyl alcohol; oleyl alcohol; isocetyl alcohol; isostearyl alcohol; and mixtures thereof.
4. The hair care composition of claim 1 , wherein the liquid fatty alcohol is selected from the group consisting of: lauryl alcohol; and a mixture of lauryl alcohol and myristyl alcohol.
5. The hair care composition of claim 1 , wherein the base oil consisting of: an isoparaffin, a mineral oil, and mixtures thereof.
6. The hair care composition of claim 1 further comprising a non-volatile silicone conditioning agent.
7. The hair care composition of claim 1 wherein the composition is substantially free of surfactants.
8. The hair care composition of claim 1 , wherein the composition is for leave-on use.
9. The hair care composition of claim 1 , wherein the composition has a turbidity of 2.0NTU or less at 25° C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/482,213 US20120308505A1 (en) | 2011-06-03 | 2012-05-29 | Clear Hair Care Composition Comprising Base Oil and Hydrophilic Component |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161492843P | 2011-06-03 | 2011-06-03 | |
| US13/482,213 US20120308505A1 (en) | 2011-06-03 | 2012-05-29 | Clear Hair Care Composition Comprising Base Oil and Hydrophilic Component |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20120308505A1 true US20120308505A1 (en) | 2012-12-06 |
Family
ID=46197737
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/482,213 Abandoned US20120308505A1 (en) | 2011-06-03 | 2012-05-29 | Clear Hair Care Composition Comprising Base Oil and Hydrophilic Component |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20120308505A1 (en) |
| EP (1) | EP2713995B1 (en) |
| JP (1) | JP5848444B2 (en) |
| CN (1) | CN103957871B (en) |
| BR (1) | BR112013030450B1 (en) |
| MX (1) | MX2013014020A (en) |
| WO (1) | WO2012166698A2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20140356308A1 (en) * | 2013-05-30 | 2014-12-04 | The Procter & Gamble Company | Non-aqueous hair oil composition comprising isoparaffin base oil, silicone elastomer and its solubilizer |
| WO2024119299A1 (en) * | 2022-12-05 | 2024-06-13 | Momentive Performance Materials Inc. | Personal care composition comprising a volatile alkane mixture and crosslinked elastomers |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6242509B1 (en) * | 1996-10-18 | 2001-06-05 | International Paper Company | Gels including bioactive components |
| US20030082129A1 (en) * | 2001-08-07 | 2003-05-01 | Buckingham Anne Marie | Hair and skin care compositions containing siloxane-based polyamide copolymers |
| US20030108504A1 (en) * | 2000-05-30 | 2003-06-12 | The Procter & Gamble Company | Hair conditioning composition comprising silicones and frizz control agents |
| US20050063934A1 (en) * | 2003-09-24 | 2005-03-24 | The Procter & Gamble Company | Conditioning composition comprising aminosilicone |
| US20060078524A1 (en) * | 2004-10-08 | 2006-04-13 | Sanjeev Midha | Multi phase personal care composition comprising a conditioning phase and an oil continuous benefit phase |
| WO2009130704A1 (en) * | 2008-04-24 | 2009-10-29 | Technion Research And Development Foundation Ltd. | Beta-lactoglobulin-polysaccharide nanoparticles for hydrophobic bioactive compounds |
| US20110311471A1 (en) * | 2010-06-22 | 2011-12-22 | Nobuaki Uehara | Clear Leave-On Hair Care Composition Comprising Aminosilicone and Its Solvent |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US824353A (en) * | 1905-07-31 | 1906-06-26 | American Suction Gas Producer Company | Gas-producer. |
| JPH02172905A (en) * | 1988-12-26 | 1990-07-04 | Mandamu:Kk | Hair cosmetic composition |
| AU4221096A (en) | 1996-01-30 | 1997-08-07 | Procter & Gamble Company, The | Hair and scalp treating compositions |
| AU2001214602A1 (en) * | 2000-05-30 | 2001-12-11 | The Procter And Gamble Company | Hair conditioning composition comprising silicones and frizz control agents |
| JP4104296B2 (en) | 2001-03-29 | 2008-06-18 | 三菱鉛筆株式会社 | Liquid oily cosmetics |
| US6979438B2 (en) * | 2002-01-25 | 2005-12-27 | The Procter & Gamble Company | Antiperspirant compositions containing petrolatum |
| US20050152539A1 (en) * | 2004-01-12 | 2005-07-14 | Brickell Ernie F. | Method of protecting cryptographic operations from side channel attacks |
| JP4351971B2 (en) * | 2004-08-31 | 2009-10-28 | ホーユー株式会社 | Oily hair cosmetic composition |
| EP2392314B1 (en) * | 2009-01-30 | 2019-08-14 | Kokyu Alcohol Kogyo Co., Ltd. | Oily hair cosmetic |
| US8562957B2 (en) * | 2009-01-30 | 2013-10-22 | Kokyu Alcohol Kogyo Co., Ltd. | Oily hair cosmetics |
-
2012
- 2012-05-29 MX MX2013014020A patent/MX2013014020A/en unknown
- 2012-05-29 US US13/482,213 patent/US20120308505A1/en not_active Abandoned
- 2012-05-29 CN CN201280026915.9A patent/CN103957871B/en active Active
- 2012-05-29 BR BR112013030450-2A patent/BR112013030450B1/en active IP Right Grant
- 2012-05-29 WO PCT/US2012/039809 patent/WO2012166698A2/en not_active Ceased
- 2012-05-29 JP JP2014513635A patent/JP5848444B2/en active Active
- 2012-05-29 EP EP12724846.6A patent/EP2713995B1/en not_active Not-in-force
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6242509B1 (en) * | 1996-10-18 | 2001-06-05 | International Paper Company | Gels including bioactive components |
| US20030108504A1 (en) * | 2000-05-30 | 2003-06-12 | The Procter & Gamble Company | Hair conditioning composition comprising silicones and frizz control agents |
| US20030082129A1 (en) * | 2001-08-07 | 2003-05-01 | Buckingham Anne Marie | Hair and skin care compositions containing siloxane-based polyamide copolymers |
| US20050063934A1 (en) * | 2003-09-24 | 2005-03-24 | The Procter & Gamble Company | Conditioning composition comprising aminosilicone |
| US8017108B2 (en) * | 2003-09-24 | 2011-09-13 | The Procter & Gamble Company | Conditioning composition comprising aminosilicone |
| US20060078524A1 (en) * | 2004-10-08 | 2006-04-13 | Sanjeev Midha | Multi phase personal care composition comprising a conditioning phase and an oil continuous benefit phase |
| WO2009130704A1 (en) * | 2008-04-24 | 2009-10-29 | Technion Research And Development Foundation Ltd. | Beta-lactoglobulin-polysaccharide nanoparticles for hydrophobic bioactive compounds |
| US20110311471A1 (en) * | 2010-06-22 | 2011-12-22 | Nobuaki Uehara | Clear Leave-On Hair Care Composition Comprising Aminosilicone and Its Solvent |
Non-Patent Citations (4)
| Title |
|---|
| International Flora Technologies, Hydrophile-Lipophile balance system, 2009, pp. 1-4 * |
| Mason et al. (Nanoemulsions: formation, structure and physical properties, J. Phys.: Condens. Matter, 2006, vol. 18, R636 2nd para.; R644, 4th para.; R-659, 3rd para. * |
| Remington Essentials of Pharmaceutics, 2012, p. 339-341 * |
| Schuller, Conditioning agents for hair and skin, CRC Press, 1999, pp. 173 * |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5848444B2 (en) | 2016-01-27 |
| WO2012166698A3 (en) | 2014-07-17 |
| EP2713995B1 (en) | 2016-08-03 |
| JP2014527507A (en) | 2014-10-16 |
| CN103957871A (en) | 2014-07-30 |
| CN103957871B (en) | 2017-04-05 |
| WO2012166698A2 (en) | 2012-12-06 |
| BR112013030450A2 (en) | 2016-09-06 |
| BR112013030450B1 (en) | 2018-05-22 |
| EP2713995A2 (en) | 2014-04-09 |
| MX2013014020A (en) | 2014-01-23 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2714199B1 (en) | Clear hair care composition comprising base oil and silicone | |
| KR920005806B1 (en) | Hair conditioning compositions | |
| EP2928563B1 (en) | Composition comprising a silicone resin and a silicone gum, personal care products containing the same | |
| US12138336B2 (en) | Personal care composition comprising water insoluble solid organic compound | |
| US20060078529A1 (en) | Hair conditioning composition comprising alkyl diquaternized ammonium salt cationic surfactant | |
| US20070190009A1 (en) | Hair Cosmetic Composition | |
| KR102376269B1 (en) | Composition for conditioning hair | |
| US20080050330A1 (en) | Aqueous hair cosmetic composition | |
| JP2002500173A (en) | Hair conditioning composition | |
| EP1267804A2 (en) | Hair care compositions containing selected frizz control agents | |
| US20030133899A1 (en) | Personal cleansing compositions that contain surfactants, co-surfactants, water insoluble solids and/or liquids and cationic conditioning polymers | |
| US20020081274A1 (en) | Personal cleansing compositions that contain surfactants, co-surfactants, water insoluble solids and/or liquids and cationic conditioning polymers | |
| US9248081B2 (en) | Clear leave-on hair care composition comprising aminosilicone and its solvent | |
| US20120308505A1 (en) | Clear Hair Care Composition Comprising Base Oil and Hydrophilic Component | |
| GB2592722A (en) | Anhydrous agent for treating keratin fibres | |
| JP6204578B2 (en) | Non-aqueous hair oil composition comprising isoparaffin base oil, silicone elastomer, and solubilizer | |
| JP2006315986A (en) | Hair cosmetic | |
| KR20090095344A (en) | Hair conditioning composition | |
| HK1189847B (en) | Clear leave-on hair care composition comprising aminosilicone and its solvent |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: THE PROCTER & GAMBLE COMPANY, OHIO Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HASEGAWA, JUN NMN;UEHARA, NOBUAKI NMN;OKU, TAISUKE NMN;REEL/FRAME:028685/0675 Effective date: 20120530 |
|
| STPP | Information on status: patent application and granting procedure in general |
Free format text: NON FINAL ACTION MAILED |
|
| STPP | Information on status: patent application and granting procedure in general |
Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER |
|
| STPP | Information on status: patent application and granting procedure in general |
Free format text: FINAL REJECTION MAILED |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |